Karina Lezirovitz

907 total citations
39 papers, 503 citations indexed

About

Karina Lezirovitz is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Karina Lezirovitz has authored 39 papers receiving a total of 503 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Sensory Systems, 20 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Karina Lezirovitz's work include Hearing, Cochlea, Tinnitus, Genetics (21 papers), Connexins and lens biology (6 papers) and Hearing Loss and Rehabilitation (5 papers). Karina Lezirovitz is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (21 papers), Connexins and lens biology (6 papers) and Hearing Loss and Rehabilitation (5 papers). Karina Lezirovitz collaborates with scholars based in Brazil, United States and France. Karina Lezirovitz's co-authors include Regina Célia Mingroni‐Netto, Ana Carla Batissoco, Paulo Alberto Otto, Jihane Romanos, Fernando Kok, Jeanne Oiticica, Ricardo Ferreira Bento, Mayana Zatz, Silvana Santos and Lúcia Inês Macedo‐Souza and has published in prestigious journals such as Annals of Neurology, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Karina Lezirovitz

35 papers receiving 497 citations

Peers

Karina Lezirovitz
MB Petersen Greece
PJ Willems Greece
Hong-Joon Park South Korea
Suoqiang Zhai China
Kotaro Ishikawa Japan
Heping Yu United States
Kärin Halsey United States
Achih Chen United States
Sébastien Chardenoux France
MB Petersen Greece
Karina Lezirovitz
Citations per year, relative to Karina Lezirovitz Karina Lezirovitz (= 1×) peers MB Petersen

Countries citing papers authored by Karina Lezirovitz

Since Specialization
Citations

This map shows the geographic impact of Karina Lezirovitz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Karina Lezirovitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karina Lezirovitz more than expected).

Fields of papers citing papers by Karina Lezirovitz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karina Lezirovitz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Karina Lezirovitz. The network helps show where Karina Lezirovitz may publish in the future.

Co-authorship network of co-authors of Karina Lezirovitz

This figure shows the co-authorship network connecting the top 25 collaborators of Karina Lezirovitz. A scholar is included among the top collaborators of Karina Lezirovitz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karina Lezirovitz. Karina Lezirovitz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bertola, Débora Romeo, et al.. (2024). Genetic heterogeneity in autosomal recessive hearing loss: a survey of Brazilian families. Frontiers in Genetics. 15. 1409306–1409306.
2.
Chen, Han, Qinghua Fang, Jakob Neef, et al.. (2023). Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing. Protein & Cell. 15(4). 305–312. 5 indexed citations
3.
Lezirovitz, Karina, et al.. (2022). Hearing aid effectiveness on patients with chronic tinnitus and associated hearing loss. Brazilian Journal of Otorhinolaryngology. 88. S164–S170. 2 indexed citations
4.
Lezirovitz, Karina & Regina Célia Mingroni‐Netto. (2021). Genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics. 141(3-4). 539–581. 8 indexed citations
5.
Shen, Jun, Beatriz R. Versiani, Robert Pogue, et al.. (2018). Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing. Hearing Research. 370. 181–188. 7 indexed citations
6.
Ballesteros, Ángela, Runjia Cui, Guilherme Lopes Yamamoto, et al.. (2018). Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific Reports. 8(1). 8706–8706. 22 indexed citations
7.
Lezirovitz, Karina, et al.. (2018). Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects. BMC Medical Genetics. 19(1). 73–73. 15 indexed citations
8.
Lezirovitz, Karina, et al.. (2017). Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2. Clinics. 72(11). 714–717. 4 indexed citations
9.
Freitas, Érika L., Karina Lezirovitz, Jeanne Oiticica, et al.. (2015). Novel partial duplication ofEYA1causes branchiootic syndrome in a large Brazilian family. International Journal of Audiology. 54(9). 593–598. 7 indexed citations
10.
Lezirovitz, Karina, et al.. (2013). 7q36 deletion and 9p22 duplication: effects of a double imbalance. Molecular Cytogenetics. 6(1). 2–2. 7 indexed citations
11.
12.
Lezirovitz, Karina, et al.. (2012). MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization. Clinics. 67(8). 981–985. 6 indexed citations
13.
Oiticica, Jeanne, Ana Carla Batissoco, Karina Lezirovitz, et al.. (2010). Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea. Journal of Translational Medicine. 8(1). 119–119. 15 indexed citations
14.
Romanos, Jihane, et al.. (2009). Novel OTOF mutations in Brazilian patients with auditory neuropathy. Journal of Human Genetics. 54(7). 382–385. 49 indexed citations
15.
Macedo‐Souza, Lúcia Inês, Fernando Kok, Silvana Santos, et al.. (2009). Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes. Annals of Human Genetics. 73(3). 382–387. 27 indexed citations
16.
Lezirovitz, Karina, et al.. (2008). Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance. Brazilian Journal of Otorhinolaryngology. 74(5). 786–789. 6 indexed citations
17.
18.
Lezirovitz, Karina, et al.. (2007). Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness. European Journal of Human Genetics. 16(1). 89–96. 46 indexed citations
19.
Lezirovitz, Karina, et al.. (2006). Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”?. Journal of Human Genetics. 51(8). 716–720. 14 indexed citations
20.
Macedo‐Souza, Lúcia Inês, Fernando Kok, Silvana Santos, et al.. (2005). Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13. Annals of Neurology. 57(5). 730–737. 47 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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